Canonical Allele Identifier: CA379959321

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32414265T>A (hg19) ; chr11:g.32392719T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392719T>A , CM000673.2:g.32392719T>A	GRCh38
NC_000011.9:g.32414265T>A , CM000673.1:g.32414265T>A	GRCh37
NC_000011.8:g.32370841T>A	NCBI36
NG_009272.1:g.47823A>T , LRG_525:g.47823A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1250A>T	ENSP00000331327.5:p.Glu417Val
ENST00000379077.9:c.*485A>T	ENSP00000368368.5:n.*485A>T
ENST00000379079.8:c.650A>T	ENSP00000368370.2:p.Glu217Val
ENST00000448076.9:c.1301A>T	ENSP00000413452.5:p.Glu434Val
ENST00000452863.10:c.1301A>T MANE Select	ENSP00000415516.5:p.Glu434Val
ENST00000526685.2:n.755A>T
ENST00000639563.3:c.1250A>T	ENSP00000492269.3:p.Glu417Val
ENST00000639907.2:n.444A>T
ENST00000640146.2:c.626A>T	ENSP00000491984.2:p.Glu209Val
ENST00000650745.1:n.510A>T
ENST00000650861.1:n.1882A>T
ENST00000651459.1:c.72A>T
ENST00000651533.1:n.347A>T
ENST00000651668.1:n.238A>T
ENST00000651794.1:n.1144A>T
ENST00000651819.1:n.226A>T
ENST00000652579.1:n.561A>T
ENST00000652724.1:n.491A>T
ENST00000332351.7:c.1286A>T	ENSP00000331327.3:p.Glu429Val
ENST00000379077.7:c.*485A>T	ENSP00000368368.3:n.*485A>T
ENST00000379079.6:c.650A>T	ENSP00000368370.2:p.Glu217Val
ENST00000448076.7:c.1286A>T	ENSP00000413452.3:p.Glu429Val
ENST00000452863.7:c.1235A>T	ENSP00000415516.3:p.Glu412Val
ENST00000527882.5:c.321-655A>T
ENST00000530998.5:c.599A>T	ENSP00000435307.1:p.Glu200Val
NM_000378.4:c.1235A>T	NP_000369.3:p.Glu412Val
NM_001198551.1:c.650A>T , LRG_525t2:c.650A>T	NP_001185480.1:p.Glu217Val
NM_001198552.1:c.599A>T	NP_001185481.1:p.Glu200Val
NM_024424.3:c.1286A>T	NP_077742.2:p.Glu429Val
NM_024426.4:c.1286A>T	NP_077744.3:p.Glu429Val
NM_000378.5:c.1250A>T	NP_000369.4:p.Glu417Val
NM_024424.4:c.1301A>T	NP_077742.3:p.Glu434Val
NM_024426.5:c.1301A>T	NP_077744.4:p.Glu434Val
NM_001367854.1:c.113A>T	NP_001354783.1:p.Glu38Val
NR_160306.1:n.1633A>T
NM_000378.6:c.1250A>T	NP_000369.4:p.Glu417Val
NM_001198552.2:c.599A>T	NP_001185481.1:p.Glu200Val
NM_024424.5:c.1301A>T	NP_077742.3:p.Glu434Val
NM_024426.6:c.1301A>T MANE Select	NP_077744.4:p.Glu434Val